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US5034160A - Sprayable fireproofing composition - Google Patents

Sprayable fireproofing composition Download PDF

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Publication number
US5034160A
US5034160A US07/535,634 US53563490A US5034160A US 5034160 A US5034160 A US 5034160A US 53563490 A US53563490 A US 53563490A US 5034160 A US5034160 A US 5034160A
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percent
composition
weight percent
clay
fibrous material
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US07/535,634
Inventor
Lawrence J. Kindt
James M. Gaidis
Joseph M. Daly
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WR Grace and Co Conn
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WR Grace and Co Conn
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Application filed by WR Grace and Co Conn filed Critical WR Grace and Co Conn
Priority to US07/535,634 priority Critical patent/US5034160A/en
Priority to CA 2027318 priority patent/CA2027318C/en
Assigned to W. R. GRACE & CO.-CONN. reassignment W. R. GRACE & CO.-CONN. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: DALY, JOSEPH M., GAIDIS, JAMES M., KINDT, LAWRENCE J.
Priority to ES91305160T priority patent/ES2075935T3/en
Priority to DE69112290T priority patent/DE69112290T2/en
Priority to EP19910305160 priority patent/EP0461821B1/en
Priority to JP16244691A priority patent/JPH0662325B2/en
Priority to AU78271/91A priority patent/AU634692B2/en
Priority to MYPI91001034A priority patent/MY106678A/en
Priority to KR1019910009698A priority patent/KR0172125B1/en
Publication of US5034160A publication Critical patent/US5034160A/en
Application granted granted Critical
Priority to HK182295A priority patent/HK182295A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/18Fireproof paints including high temperature resistant paints
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/14Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing calcium sulfate cements
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D1/00Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
    • C09D1/06Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances cement
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/02Inorganic materials
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/44Thickening, gelling or viscosity increasing agents
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00034Physico-chemical characteristics of the mixtures
    • C04B2111/00146Sprayable or pumpable mixtures
    • C04B2111/00155Sprayable, i.e. concrete-like, materials able to be shaped by spraying instead of by casting, e.g. gunite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00482Coating or impregnation materials
    • C04B2111/00525Coating or impregnation materials for metallic surfaces
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/20Resistance against chemical, physical or biological attack
    • C04B2111/28Fire resistance, i.e. materials resistant to accidental fires or high temperatures
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Definitions

  • the subject invention is directed to coating compositions which are applicable in the field of construction materials.
  • the invention is particularly applicable to the field of high-rise construction based on steel infrastructure where it is desired to provide fireproofing and/or acoustical insulation.
  • Thick coatings of inorganic materials have been commonly applied in the course of the erection of steel structures designed to serve as multi-story building infrastructure primarily to serve in a fireproofing capacity, as well as to function as acoustic insulation agents. In the event of a major fire in a section or on one or more floors of a building, it has been found that such coatings substantially inhibit thermal weakening of the steel infrastructure and, thus, prevent a catastrophic collapse of the building.
  • coating mixes both in the wet and dry state, must possess a number of crucial properties. They must be able to hold the large quantity of water that renders them capable of being pumped easily and to great heights. Although high water content is desired, the aqueous dispersion must retain a consistency sufficient to prevent segregation or settling of ingredients and permit adequate "yield" or uniform coverage on the steel surface at a given thickness. Furthermore, the coating mixtures must obviously be capable of adhering to steel surfaces, both in the slurried state and upon drying. Finally, the mixtures must set without any undue expansion or shrinkage which could result in the formation of cracks that would seriously detract from the insulating value of the dry coating.
  • compositions containing synthetic and natural organic particulate material have been suggested (See U.S. Pat. No. 4,751,024). Due to the hydrophobic nature of the organic material, the composition's properties are very sensitive to the water content used in forming the sprayable mix. Thus, when a low water content is used, it is difficult to form a uniform fluid mixture which is capable of being readily pumped to the desired point of application. When the water content is increased to achieve a mixture of lower viscosity (and thus readily mixable and pumpable), the resultant mixture exhibits a high flow at the point of application and, thus, does not readily maintain its shape and adhere to the infrastructural surface. Such formulations may fall off at the surface and, thereby, lose the advantages achievable by the coating.
  • thicken formulations e.g. polyethylene oxide, xanthan gum, carboxymethyl cellulose guar gum, hydroxypropyl guar gum.
  • agents may provide a less fluid composition at the point of application and thereby aid in initial adhesion, they are not desirable for the instant application as they impair the ability of providing a uniform initial mix and require more energy (larger pumps) to force the fluid through the conduit to the point of application.
  • thickeners in many instances, do not impart good adhesion properties to compositions containing them.
  • agents are known to impart thixotropic properties to fluids. These agents include attapulgite and sepiolite clays which are conventionally provided as ultrafine colloidal material.
  • attapulgite and sepiolite clays which are conventionally provided as ultrafine colloidal material.
  • JP 63-297256 teaches the use of sepiolite as a thixotropy-imparting agent for an inorganic adhesive spray composition.
  • thixotropic agents would detract from the instant formulation. They would provide high viscosity under the low shear mixing conditions. The formulator would not be able to provide a uniform composition or would be required to add excess water at the mixing stage which would cause a high flow coating to be applied.
  • the present invention is directed to enhanced fireproofing spray compositions which, when initially mixed with water, exhibit low viscosity while, after subjection to high shear, exhibit higher viscosity.
  • the mixture is thus readily formed into an aqueous dispersion which, upon application, exhibits minimal flow and good adhesion to the structural substrate.
  • the composition comprises a hydratable cement binder, a porous aggregate, a fibrous material in combination with a magnesium silicate-based clay selected from attapulgite, sepiolite or mixtures thereof wherein the clay has a particle size distribution such that the average particle size is at least 74 microns and that at least 60 weight percent is of a particle size of at least 44 microns or larger.
  • rheopectic shall mean compositions which, when presented in a fluid state, are capable of exhibiting an increase in viscosity after application of shear forces to the fluid.
  • thixotropic shall refer to compositions which, when presented in a fluid state, are capable of exhibiting a decrease in viscosity upon application of shear forces to the fluid.
  • Rheopectic and thixotropic fluids are both classified as viscosity time-dependent-under-shear fluids but exhibit viscosity properties which are substantially opposite to each other.
  • the present invention is directed to a novel composition suitable for spray application onto steel infrastructures and other substructures of buildings to provide fireproofing and acoustical dampening.
  • the subject compositions are capable of exhibiting a low initial viscosity (high fluidity) and, after subjection to high shear force, exhibiting a high viscosity.
  • the compositions have unexpectedly been found to be capable of being readily mixed using conventional mixing apparatus without the concern for criticality of water to solid content (within conventional ranges) and to be capable of providing a product which exhibits a high yield coating which has the ability to adhere and maintain itself as a coating on the substructure surface.
  • the subject composition comprises a hydratable cementitious binder, a porous aggregate, an air-entraining agent, a fibrous material and a magnesium silicate-based clay selected from attapulgite, sepiolite or mixtures thereof composed of large particle size (diameter) material.
  • the present invention is directed to fireproofing coating such as disclosed in U.S. Pat. Nos. 3,719,513, 3,839,059 (exfoliated vermiculite-based compositions) and 4,751,024 (polystyrene-based compositions) which have been enhanced and improved by the addition of the presently described magnesium silicate clay to impart rheopectic properties to the resultant composition.
  • the teachings of U.S. Pat. Nos. 3,719,513; 3,839,059; and 4,751,024 are expressly incorporated herein by reference.
  • the present invention is a cementitious composition. It requires the use of from about 50 to 90 weight percent of a hydratable cementitious binder.
  • a hydratable cementitious binder also known as gypsum plaster or plaster of paris
  • the binder can be used in relatively low amounts, e.g. as little as 50 percent by weight. It is generally preferred to employ from about 50 to 70, preferably 50 to 60, weight percent binder when the aggregate is a relatively high density (e.g. 2-12 lbs/ft 2 ) aggregate (i.e. vermiculite or perlite or mixtures thereof).
  • the aggregate is a relatively low density aggregate (0.3-1 lb/ft 2 ) (i.e. polystyrene).
  • the porous aggregate of the present composition can be selected from vermiculite, perlite or shredded polystyrene (preferred).
  • the aggregate is normally contained in the subject composition in a volume percent concentration of from about 3 to 40 with amounts of from about 3 to 20 volume percent being preferred.
  • Low density aggregate is preferred as it provides a higher volume coating per unit weight of total composition.
  • the particle size at its maximum dimension is less than 1/4 inch.
  • vermiculite aggregate normally used is exfoliated (expanded) vermiculite of standard grade having a density of about 5-7 pounds per cu. foot.
  • Prior fireproofing compositions formed with vermiculite as the porous particulate have exhibited characteristics which tend to vary from batch to batch due to the variations in this natural product.
  • the incorporation of the presently described rheopectic agent overcomes such variations and thus, provides an improved composition.
  • perlite is essentially an amorphous mineral composed of fused sodium potassium aluminum silicate. The mineral is conventionally ground and then expanded by heating to form particulate material having densities ranging from about 2 to 12 pounds per cubic foot. Preferred perlite aggregates are commercial grades of expanded perlite having a density of from 2 to 5 lbs/cu. ft.
  • the use of the subject rheopectic agents is particularly useful in combination with perlite containing compositions as such compositions tend to be too fluid at the point of application to provide good adhesion.
  • the subject rheopectic agents provide a counteracting property which enhances conventional perlite compositions to achieve the desired properties both during mixing and at the point of application.
  • the preferred porous aggregate used in the present coating compositions is shredded polystyrene particles which can be produced by shredding loose expanded polystyrene beads or molded polystyrene beadboard. Extruded polystyrene can also be shredded to provide the aggregate material of this invention.
  • a method and apparatus for shredding foamed polystyrene beads are disclosed in U.S. Pat. Nos. 3,627,211, and 3,686,068 the disclosure of which is expressly incorporated by reference herein. As disclosed in these patents, the shredded particles have irregularly shaped exterior surfaces, tears, and ragged edges.
  • the shredding process opens a substantial number of the cells on the surface of the foamed beads, thereby allowing penetration of the cementitious binder into the cellular structure and integrating the binder and the particles.
  • the density of the shredded polystyrene is preferably in the range of about 0.3 to 0.8 pounds per cubic foot, more preferably about 0.4 to 0.6 pcf.
  • the aggregate is contained in the subject composition to aid in providing a high yield coating.
  • the amount of aggregate used (in terms of weight percent) will be, generally, directly proportional to the density of the aggregate.
  • the vermiculite is used in from about 20 to 40, preferably 30 to 40 weight percent of the composition.
  • shredded polystyrene density of about 0.2 to 0.8 lbs/ft 3
  • this aggregate is used in from about 1 to 5, preferably about 1 to 3 weight percent of the composition.
  • perlite When perlite is the aggregate of the composition (density ranges from 2 to 12 lbs/ft 3 ), the perlite should be present in from about 5 to 40 weight percent. Low density perlite (2-5 lbs/ft 3 ) is normally present in from about 5 to 30 weight percent while high density perlite (7-12 lbs/ft 3 ), when used, is present in from about 20 to 40 weight percent.
  • the volume of aggregate contained in a 100 pounds of composition is from about 2 to 10 cubic feet, preferably from about 4 to 8 cubic feet.
  • the fibrous component of the present composition is normally provided by either organic fibrous material alone or in combination with inorganic fibrous material.
  • the organic fibrous material is a high wet bulking organic fiber, such as cellulose fibers described in U.S. Pat. Nos. 3,719,513 and 3,839,059.
  • the inorganic fibers should be capable of providing reinforcement of the composition, and are preferably glass fibers.
  • the total amount of fibrous component is from about 4 to 12 weight percent of the composition with the organic fibers being from about 4 to 10 weight percent and the inorganic fibers, when present, being present in from 0 to about 2 weight percent.
  • the foaming agents or air entraining agents that are used in the compositions of this invention are well-known in the cement art.
  • Such well-known materials as sulfonated monoglycerides, sodium alkyl arylsulfonate, and sodium lauryl sulfate, can be used in appropriate quantities to provide a slurry of desired density and pumpability.
  • Dry foaming agents can be incorporated into the dry composition before addition of water, while both dry and liquid agents can be added to the slurried composition.
  • the air-entraining agent may be present in from 0.05 to about 0.5% by weight with from 0.1% to 0.5% by weight, preferred.
  • the subject compositions must contain certain specific material, as fully described below, to impart rheopectic properties to the aqueous dispersion of the composition.
  • These materials are attapulgite, sepiolite and mixtures thereof which are of relatively large particle size.
  • Attapulgite or Attapulgus clay is an off-white or cream-colored needle-like crystal normally mined in Attapulgus, Ga., and parts of Florida. Sepiolite (meershaum) occurs in California, U.S.A. as well as in parts of Turkey, Spain, Greece and Sydney. In both instances, the mined material is dried to remove the free water. The dried product is initially broken into a tough, granulated "first cut" material which is then subjected to ball milling or the like to form very fine particulate powder. The resultant very fine powder (90% or greater amount has particle size of less than 44 microns) product is conventionally used as a thixotropic agent in paints, inks, adhesives and the like.
  • the attapulgite and sepiolite material found useful herein are the granular particles which have a particle size distribution such that at least 60 percent by weight (preferably at least 80 percent by weight) is of a particle size of at least 44 microns or greater (is retained on a No. 325 mesh screen of U.S. Standard Sieve Series).
  • the average particle size should be at least 74 microns or greater, (retained on a No. 200 mesh sieve).
  • the particles can have a particle size distribution such that at least about 60% of the sepiolite particles are of 44 microns or larger.
  • the subject attapulgite and sepiolite are obtainable as first cut material.
  • the particle size distribution has a major amount of material which is +100 mesh and most preferably +50 mesh (297 microns or greater). Particles greater than +10 mesh (2000 microns) are not desired.
  • the subject attapulgite and sepiolite have low moisture content.
  • the moisture content should be less than about 16%, with from about 4 to 16 percent being preferred and from about 4 to 10 percent being most preferred.
  • the preferred clays are dried at low temperatures (50° to 250° F.) to reduce the moisture content.
  • Attapulgite and sepiolite granular material has unexpectedly been found to cause the desired rheopectic property to be imparted to aqueous dispersions of the subject composition.
  • other clays such as bentonite, kaolin as well as fine particulate (normally less than 44 micron) attapulgite and sepiolite powders do not provide the desired property.
  • the subject composition should contain a sufficient amount of the above-described course particulate clay to impart rheopectic properties to the resultant aqueous dispersion. Minimal experimentation will determine the exact amount needed for a particular formulation. It is normally desirable to use from 3 to 20 weight percent, preferably from 3 to 10 weight percent of the granular attapulgite, sepiolite or mixture thereof to provide the enhanced formulation.
  • an aqueous composition exhibit relatively low viscosity at the low shear mixing stage but significantly higher viscosity subsequent to being subjected to high shear forces of the pump and spray apparatus.
  • the subject compositions are capable of providing an aqueous dispersion which is not sensitive to normal deviations in water content, are readily mixed and pumped to the application site without segregation and which provide coatings of high yield, i.e. placement over a relatively large area, per weight of the dry composition, at a given thickness of application. Yield is generally calculated by methods known in the art as board feet per dry weight of composition.
  • the particularly preferred compositions are capable of providing a high yield of at least about 20 board feet per 45 pounds by weight of the dry composition. Generally, a yield in the range of about 25 to 35 board feet per 45 pounds dry weight is obtained.
  • the subject compositions also exhibit a low flow and are, therefore, capable of being applied to vertical surfaces without sagging, run-off, or fall-off. Instead, the subject compositions adhere to the applied substructure prior to set and after set.
  • a conventional (to the cement technology) water-retaining agent which allows more water to be incorporated into the slurry, thereby increasing yield, while retaining about the same level of adhesion to steel.
  • a preferred water-retaining agent is hydroxypropylmethylcellulose.
  • the dry compositions of this invention are converted to pumpable slurries by addition of water.
  • the water is added to the dry mix at the job site shortly before being pumped to the point of application.
  • a water to cementitious binder ratio of about 1.2:1 to 2.5:1 is generally employed to provide a pumpable mixture of desired consistency and adhesiveness.
  • a useful range of slurry density, which affords easy pumping, is about 35 to 55 pounds per cubic foot (pcf).
  • compositions of the instant invention exhibit low viscosity when mixed with water under the low shear forces normally produced by conventional mixers (e.g. mortar mixers having paddle or spiral blade design or the like) to produce the coating composition at the construction or job site.
  • conventional mixers e.g. mortar mixers having paddle or spiral blade design or the like
  • the dispersion exhibits its rheopectic abilities and provides a high viscosity material.
  • the high shear is provided by standard application pumps, such as a piston pump capable of pumping the subject composition at a rate of from about 1 to 2.5 ft 3 /min.
  • Each piston normally has a piston stroke of about 4 to 5 inches in a 3 inch bore with from 50 to 125 strokes per minute (SPM) per cylinder.
  • SPM strokes per minute
  • the typical application setting is about 100 SPM which provides for a calculated volumetric output of about 1.5-2 cu.ft./min./cyl.
  • the actual volumetric output may be only 25 to 50 percent of this due to the compressible nature of the fluid composition being moved and the amount of pumping pressure being generated.
  • a gypsum-based composition was prepared by dry mixing the following ingredients:
  • the granules had a distribution of 17% of +50 mesh; 39% of +100 mesh; 31% of +200 mesh; and 13% of +325 mesh.
  • the formed dry composition was mixed with water at a water/solids ratio of 1.4 using a ribbon blade mortar mixer to provide a substantially uniform dispersion.
  • the dispersion was transported to a spray applicator using a Thompson A375 sprayer-pump of a cylinder-pump design which imparts high shear forces to the dispersion.
  • the dispersion is carried through 200 foot hose at a pump pressure of 170 psi.
  • the pumped slurry was applied to a 10-inch steel I-beam to provide an even coating of 0.75 inch thickness.
  • Viscosity measurements were made of the dispersion after mixing, after subjection to the high shear forces of the spray pump and also of the sprayed material.
  • the formed coating was observed 20 minutes after application to determine if the dispersion commenced to set and if any cracking, sagging or adhesion fault (material falls off) occurred. The results are shown below:
  • the components formed a dispersion of low viscosity in the mixer and thus was readily mixed to a uniform consistency. After subjection to the high shear forces of the pump the compositions's viscosity began to increase and became stiff after subjection to the spray-applicator. Thus, the dispersion exhibited a high degree of body which adhered well to the steel structure and did not crack or sag while setting to a dry uniform coating.
  • a gypsum-based composition was prepared by dry mixing the following:
  • Example II The dry composition was mixed, pumped, sprayed and applied in the same manner as described in Example I above except that the water/solids ratio was 1.45 and the pump pressure was 185 psi. Viscosity measurements and observations were done as described in Example I above. The results were:
  • a second composition was formed in the same manner as described above except that the sepiolite was not present.
  • the initial composition had good viscosity in the mixer but, upon application, was too thin to remain on the steel beam, e.g. it exhibited sagging and poor adhesion.
  • a dry gypsum-based composition was formed by dry mixing the following:
  • Example I The dry mixture was mixed with water (water/solid ratio of 1.7), pumped and spray-applied to a steel I-beam as described in Example I above. Vicat Viscosity measurements and observation of the formed coating were made as described in Example I above. The results are given below:
  • the higher density aggregate used here required higher loading of aggregate and, therefore, a predictably more viscous initial dispersion.
  • the material was readily mixable to a uniform dispersion which did exhibit the desired rheopectic properties after the pump and sprayer and thereby provided a coating having excellent properties.
  • a dry gypsum-based composition was formed by dry mixing the following:
  • Example 1 The dry mix was mixed with water (water/solid ratio of 1.4), pumped and spray-applied to a steel I-beam as described in Example 1 above. The following measurements and observations were made as described in Example I.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Structural Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Paints Or Removers (AREA)
  • Fireproofing Substances (AREA)
  • Medicinal Preparation (AREA)
  • Building Environments (AREA)

Abstract

A sprayable fireproofing composition comprising a hydratable cementitious binder, a porous aggregate, a fibrous material, an air-entraining agent and a rheopectic agent selected from granular attapulgite, sepiolite or mixture thereof having a major amount of particulate greater than 40 microns and water content less than 16 percent.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The subject invention is directed to coating compositions which are applicable in the field of construction materials. The invention is particularly applicable to the field of high-rise construction based on steel infrastructure where it is desired to provide fireproofing and/or acoustical insulation.
2. Description of the Related Art
Thick coatings of inorganic materials have been commonly applied in the course of the erection of steel structures designed to serve as multi-story building infrastructure primarily to serve in a fireproofing capacity, as well as to function as acoustic insulation agents. In the event of a major fire in a section or on one or more floors of a building, it has been found that such coatings substantially inhibit thermal weakening of the steel infrastructure and, thus, prevent a catastrophic collapse of the building.
In order to be suitable for such use, coating mixes, both in the wet and dry state, must possess a number of crucial properties. They must be able to hold the large quantity of water that renders them capable of being pumped easily and to great heights. Although high water content is desired, the aqueous dispersion must retain a consistency sufficient to prevent segregation or settling of ingredients and permit adequate "yield" or uniform coverage on the steel surface at a given thickness. Furthermore, the coating mixtures must obviously be capable of adhering to steel surfaces, both in the slurried state and upon drying. Finally, the mixtures must set without any undue expansion or shrinkage which could result in the formation of cracks that would seriously detract from the insulating value of the dry coating. This complex balance of properties has substantially been achieved heretofore by gypsum-vermiculite systems containing cellulosic fiber. Examples of compositions of this general type are described by Bragg in U.S. Pat. Nos. 3,719,573 and 3,839,059. However, vermiculite as a naturally occurring mineral is subject to variations in quality, uniformity and consistency.
In order to overcome the deficiencies encountered with vermiculite-based mixtures, compositions containing synthetic and natural organic particulate material have been suggested (See U.S. Pat. No. 4,751,024). Due to the hydrophobic nature of the organic material, the composition's properties are very sensitive to the water content used in forming the sprayable mix. Thus, when a low water content is used, it is difficult to form a uniform fluid mixture which is capable of being readily pumped to the desired point of application. When the water content is increased to achieve a mixture of lower viscosity (and thus readily mixable and pumpable), the resultant mixture exhibits a high flow at the point of application and, thus, does not readily maintain its shape and adhere to the infrastructural surface. Such formulations may fall off at the surface and, thereby, lose the advantages achievable by the coating.
Various agents are known to thicken formulations e.g. polyethylene oxide, xanthan gum, carboxymethyl cellulose guar gum, hydroxypropyl guar gum. Although such agents may provide a less fluid composition at the point of application and thereby aid in initial adhesion, they are not desirable for the instant application as they impair the ability of providing a uniform initial mix and require more energy (larger pumps) to force the fluid through the conduit to the point of application. Further, such thickeners, in many instances, do not impart good adhesion properties to compositions containing them.
Other agents are known to impart thixotropic properties to fluids. These agents include attapulgite and sepiolite clays which are conventionally provided as ultrafine colloidal material. For example, U.S. Pat. Nos. 3,986,969 and 4,801,395 describe the use of attapulgite as a thixotropic agent while JP 63-297256 teaches the use of sepiolite as a thixotropy-imparting agent for an inorganic adhesive spray composition. The use of thixotropic agents would detract from the instant formulation. They would provide high viscosity under the low shear mixing conditions. The formulator would not be able to provide a uniform composition or would be required to add excess water at the mixing stage which would cause a high flow coating to be applied.
It is highly desired to provide a fireproofing and acoustical dampening composition which, when initially mixed with water at the job site, exhibits low viscosity to allow the components to readily mix and form a uniform composition while being capable of exhibiting high viscosity and minimal flow at the point of application to thus maintain its shape and adherence to the applied structure.
SUMMARY OF THE INVENTION
The present invention is directed to enhanced fireproofing spray compositions which, when initially mixed with water, exhibit low viscosity while, after subjection to high shear, exhibit higher viscosity. The mixture is thus readily formed into an aqueous dispersion which, upon application, exhibits minimal flow and good adhesion to the structural substrate.
The composition comprises a hydratable cement binder, a porous aggregate, a fibrous material in combination with a magnesium silicate-based clay selected from attapulgite, sepiolite or mixtures thereof wherein the clay has a particle size distribution such that the average particle size is at least 74 microns and that at least 60 weight percent is of a particle size of at least 44 microns or larger.
DETAILED DESCRIPTION
For purposes of clarity, the following terms used in the present specification and appended claims are defined below:
The term "rheopectic" shall mean compositions which, when presented in a fluid state, are capable of exhibiting an increase in viscosity after application of shear forces to the fluid.
The term "thixotropic" shall refer to compositions which, when presented in a fluid state, are capable of exhibiting a decrease in viscosity upon application of shear forces to the fluid.
Rheopectic and thixotropic fluids are both classified as viscosity time-dependent-under-shear fluids but exhibit viscosity properties which are substantially opposite to each other.
The concentration of the components of the present composition are given herein in terms of parts by weight unless otherwise indicated.
The present invention is directed to a novel composition suitable for spray application onto steel infrastructures and other substructures of buildings to provide fireproofing and acoustical dampening. The subject compositions are capable of exhibiting a low initial viscosity (high fluidity) and, after subjection to high shear force, exhibiting a high viscosity. The compositions have unexpectedly been found to be capable of being readily mixed using conventional mixing apparatus without the concern for criticality of water to solid content (within conventional ranges) and to be capable of providing a product which exhibits a high yield coating which has the ability to adhere and maintain itself as a coating on the substructure surface.
The subject composition comprises a hydratable cementitious binder, a porous aggregate, an air-entraining agent, a fibrous material and a magnesium silicate-based clay selected from attapulgite, sepiolite or mixtures thereof composed of large particle size (diameter) material. In particular, the present invention is directed to fireproofing coating such as disclosed in U.S. Pat. Nos. 3,719,513, 3,839,059 (exfoliated vermiculite-based compositions) and 4,751,024 (polystyrene-based compositions) which have been enhanced and improved by the addition of the presently described magnesium silicate clay to impart rheopectic properties to the resultant composition. The teachings of U.S. Pat. Nos. 3,719,513; 3,839,059; and 4,751,024 are expressly incorporated herein by reference.
The present invention is a cementitious composition. It requires the use of from about 50 to 90 weight percent of a hydratable cementitious binder. Known Portland cements can be used as the binder. However, it is generally preferred to employ a hydratable gypsum binder (also known as gypsum plaster or plaster of paris) due to its advantageous fireproofing characteristics. The binder can be used in relatively low amounts, e.g. as little as 50 percent by weight. It is generally preferred to employ from about 50 to 70, preferably 50 to 60, weight percent binder when the aggregate is a relatively high density (e.g. 2-12 lbs/ft2) aggregate (i.e. vermiculite or perlite or mixtures thereof). However, it is generally preferred to employ at least about 75 percent by weight based on the total weight of the composition, and more preferably at least about 85% by weight when the aggregate is a relatively low density aggregate (0.3-1 lb/ft2) (i.e. polystyrene).
The porous aggregate of the present composition can be selected from vermiculite, perlite or shredded polystyrene (preferred). The aggregate is normally contained in the subject composition in a volume percent concentration of from about 3 to 40 with amounts of from about 3 to 20 volume percent being preferred. Low density aggregate is preferred as it provides a higher volume coating per unit weight of total composition. Preferably, the particle size at its maximum dimension is less than 1/4 inch.
The vermiculite aggregate normally used is exfoliated (expanded) vermiculite of standard grade having a density of about 5-7 pounds per cu. foot. Prior fireproofing compositions formed with vermiculite as the porous particulate have exhibited characteristics which tend to vary from batch to batch due to the variations in this natural product. The incorporation of the presently described rheopectic agent overcomes such variations and thus, provides an improved composition.
Another useful aggregate material is perlite. This material is essentially an amorphous mineral composed of fused sodium potassium aluminum silicate. The mineral is conventionally ground and then expanded by heating to form particulate material having densities ranging from about 2 to 12 pounds per cubic foot. Preferred perlite aggregates are commercial grades of expanded perlite having a density of from 2 to 5 lbs/cu. ft.
The use of the subject rheopectic agents, as fully described herein below, is particularly useful in combination with perlite containing compositions as such compositions tend to be too fluid at the point of application to provide good adhesion. The subject rheopectic agents provide a counteracting property which enhances conventional perlite compositions to achieve the desired properties both during mixing and at the point of application.
The preferred porous aggregate used in the present coating compositions is shredded polystyrene particles which can be produced by shredding loose expanded polystyrene beads or molded polystyrene beadboard. Extruded polystyrene can also be shredded to provide the aggregate material of this invention. A method and apparatus for shredding foamed polystyrene beads are disclosed in U.S. Pat. Nos. 3,627,211, and 3,686,068 the disclosure of which is expressly incorporated by reference herein. As disclosed in these patents, the shredded particles have irregularly shaped exterior surfaces, tears, and ragged edges. The shredding process opens a substantial number of the cells on the surface of the foamed beads, thereby allowing penetration of the cementitious binder into the cellular structure and integrating the binder and the particles. The density of the shredded polystyrene is preferably in the range of about 0.3 to 0.8 pounds per cubic foot, more preferably about 0.4 to 0.6 pcf.
The aggregate is contained in the subject composition to aid in providing a high yield coating. The amount of aggregate used (in terms of weight percent) will be, generally, directly proportional to the density of the aggregate. Thus, when the aggregate is exfoliated vermiculite (density of about 5-7 lbs/ft3), the vermiculite is used in from about 20 to 40, preferably 30 to 40 weight percent of the composition. When shredded polystyrene is used (density of about 0.2 to 0.8 lbs/ft3), this aggregate is used in from about 1 to 5, preferably about 1 to 3 weight percent of the composition. When perlite is the aggregate of the composition (density ranges from 2 to 12 lbs/ft3), the perlite should be present in from about 5 to 40 weight percent. Low density perlite (2-5 lbs/ft3) is normally present in from about 5 to 30 weight percent while high density perlite (7-12 lbs/ft3), when used, is present in from about 20 to 40 weight percent. In general, the volume of aggregate contained in a 100 pounds of composition is from about 2 to 10 cubic feet, preferably from about 4 to 8 cubic feet.
The fibrous component of the present composition is normally provided by either organic fibrous material alone or in combination with inorganic fibrous material. Preferably, the organic fibrous material is a high wet bulking organic fiber, such as cellulose fibers described in U.S. Pat. Nos. 3,719,513 and 3,839,059. The inorganic fibers should be capable of providing reinforcement of the composition, and are preferably glass fibers. The total amount of fibrous component is from about 4 to 12 weight percent of the composition with the organic fibers being from about 4 to 10 weight percent and the inorganic fibers, when present, being present in from 0 to about 2 weight percent.
The foaming agents or air entraining agents that are used in the compositions of this invention are well-known in the cement art. Such well-known materials as sulfonated monoglycerides, sodium alkyl arylsulfonate, and sodium lauryl sulfate, can be used in appropriate quantities to provide a slurry of desired density and pumpability. Dry foaming agents can be incorporated into the dry composition before addition of water, while both dry and liquid agents can be added to the slurried composition. The air-entraining agent may be present in from 0.05 to about 0.5% by weight with from 0.1% to 0.5% by weight, preferred.
In addition to the above-described components, the subject compositions must contain certain specific material, as fully described below, to impart rheopectic properties to the aqueous dispersion of the composition. These materials are attapulgite, sepiolite and mixtures thereof which are of relatively large particle size.
Attapulgite or Attapulgus clay is an off-white or cream-colored needle-like crystal normally mined in Attapulgus, Ga., and parts of Florida. Sepiolite (meershaum) occurs in California, U.S.A. as well as in parts of Turkey, Spain, Greece and Morocco. In both instances, the mined material is dried to remove the free water. The dried product is initially broken into a tough, granulated "first cut" material which is then subjected to ball milling or the like to form very fine particulate powder. The resultant very fine powder (90% or greater amount has particle size of less than 44 microns) product is conventionally used as a thixotropic agent in paints, inks, adhesives and the like.
The attapulgite and sepiolite material found useful herein are the granular particles which have a particle size distribution such that at least 60 percent by weight (preferably at least 80 percent by weight) is of a particle size of at least 44 microns or greater (is retained on a No. 325 mesh screen of U.S. Standard Sieve Series). The average particle size should be at least 74 microns or greater, (retained on a No. 200 mesh sieve). When attapulgite is used, it is preferred that at least about 80 percent by weight of the attapulgite particles are at least 44 microns or larger. When sepiolite granular material is used, the particles can have a particle size distribution such that at least about 60% of the sepiolite particles are of 44 microns or larger. The subject attapulgite and sepiolite are obtainable as first cut material. Preferably, the particle size distribution has a major amount of material which is +100 mesh and most preferably +50 mesh (297 microns or greater). Particles greater than +10 mesh (2000 microns) are not desired.
It is preferable that the subject attapulgite and sepiolite have low moisture content. The lower the moisture content, the greater the ability the clay has to impart rheopectic properties to aqueous dispersions of the instant composition. The moisture content should be less than about 16%, with from about 4 to 16 percent being preferred and from about 4 to 10 percent being most preferred. The preferred clays are dried at low temperatures (50° to 250° F.) to reduce the moisture content.
The presently required attapulgite and sepiolite granular material has unexpectedly been found to cause the desired rheopectic property to be imparted to aqueous dispersions of the subject composition. In contrast, other clays such as bentonite, kaolin as well as fine particulate (normally less than 44 micron) attapulgite and sepiolite powders do not provide the desired property.
The subject composition should contain a sufficient amount of the above-described course particulate clay to impart rheopectic properties to the resultant aqueous dispersion. Minimal experimentation will determine the exact amount needed for a particular formulation. It is normally desirable to use from 3 to 20 weight percent, preferably from 3 to 10 weight percent of the granular attapulgite, sepiolite or mixture thereof to provide the enhanced formulation.
This unexpected ability to impart a shear-thickening behavior is highly desired and of extreme technological utility in the process of mixing and subsequent spray application of the subject formulations onto the infrastructure of buildings. It is most desirable that an aqueous composition exhibit relatively low viscosity at the low shear mixing stage but significantly higher viscosity subsequent to being subjected to high shear forces of the pump and spray apparatus. The subject compositions are capable of providing an aqueous dispersion which is not sensitive to normal deviations in water content, are readily mixed and pumped to the application site without segregation and which provide coatings of high yield, i.e. placement over a relatively large area, per weight of the dry composition, at a given thickness of application. Yield is generally calculated by methods known in the art as board feet per dry weight of composition. The particularly preferred compositions are capable of providing a high yield of at least about 20 board feet per 45 pounds by weight of the dry composition. Generally, a yield in the range of about 25 to 35 board feet per 45 pounds dry weight is obtained. The subject compositions also exhibit a low flow and are, therefore, capable of being applied to vertical surfaces without sagging, run-off, or fall-off. Instead, the subject compositions adhere to the applied substructure prior to set and after set.
In certain instances it is also desirable to incorporate into the mix a conventional (to the cement technology) water-retaining agent which allows more water to be incorporated into the slurry, thereby increasing yield, while retaining about the same level of adhesion to steel. A preferred water-retaining agent is hydroxypropylmethylcellulose.
The dry compositions of this invention are converted to pumpable slurries by addition of water. Generally, the water is added to the dry mix at the job site shortly before being pumped to the point of application. A water to cementitious binder ratio of about 1.2:1 to 2.5:1 is generally employed to provide a pumpable mixture of desired consistency and adhesiveness. Generally, a useful range of slurry density, which affords easy pumping, is about 35 to 55 pounds per cubic foot (pcf).
The compositions of the instant invention exhibit low viscosity when mixed with water under the low shear forces normally produced by conventional mixers (e.g. mortar mixers having paddle or spiral blade design or the like) to produce the coating composition at the construction or job site. When the resultant aqueous dispersion is subjected to high shear forces, such as is generated by piston pumps used to move and supply the aqueous composition to the site of application, the dispersion exhibits its rheopectic abilities and provides a high viscosity material. The high shear is provided by standard application pumps, such as a piston pump capable of pumping the subject composition at a rate of from about 1 to 2.5 ft3 /min. Each piston normally has a piston stroke of about 4 to 5 inches in a 3 inch bore with from 50 to 125 strokes per minute (SPM) per cylinder. The typical application setting is about 100 SPM which provides for a calculated volumetric output of about 1.5-2 cu.ft./min./cyl. The actual volumetric output may be only 25 to 50 percent of this due to the compressible nature of the fluid composition being moved and the amount of pumping pressure being generated.
The following examples are given for illustrative purposes only and are not meant to be a limitation on the appended claims. All parts and percentages are by weight unless otherwise indicated.
EXAMPLE I
A gypsum-based composition was prepared by dry mixing the following ingredients:
______________________________________                                    
Ingredient         wt. %                                                  
______________________________________                                    
Gypsum Plaster     82.5                                                   
Shredded Expanded  2.9                                                    
Polystyrene (0.375 pcf)                                                   
Cellulose fiber    6.2                                                    
Air-entraining agent                                                      
                   0.2                                                    
(alpha-olefinsulfonate)                                                   
(WITCONATE AOK)                                                           
Attapulgite granules                                                      
                   8.2                                                    
(90+ % greater than                                                       
325 mesh U.S. Std.;                                                       
Average Particle Size of                                                  
140 mesh)                                                                 
______________________________________                                    
The granules had a distribution of 17% of +50 mesh; 39% of +100 mesh; 31% of +200 mesh; and 13% of +325 mesh.
The formed dry composition was mixed with water at a water/solids ratio of 1.4 using a ribbon blade mortar mixer to provide a substantially uniform dispersion. The dispersion was transported to a spray applicator using a Thompson A375 sprayer-pump of a cylinder-pump design which imparts high shear forces to the dispersion. The dispersion is carried through 200 foot hose at a pump pressure of 170 psi. The pumped slurry was applied to a 10-inch steel I-beam to provide an even coating of 0.75 inch thickness. Viscosity measurements were made of the dispersion after mixing, after subjection to the high shear forces of the spray pump and also of the sprayed material. The formed coating was observed 20 minutes after application to determine if the dispersion commenced to set and if any cracking, sagging or adhesion fault (material falls off) occurred. The results are shown below:
______________________________________                                    
Viscosity.sup.1                                                           
               Observations                                               
Mixer Pump    Sprayer  Set.sup.2                                          
                            Cracking                                      
                                   Sagging                                
                                          Adhesion                        
______________________________________                                    
27    21      16       Yes  No     No     Yes                             
______________________________________                                    
 .sup.1 Done according to ASTM C472 using Vicat Viscometer adapted for    
 sanded plaster. Low numbers indicate high viscosity.                     
 .sup.2 Observation taken at 6 hours.                                     
The components formed a dispersion of low viscosity in the mixer and thus was readily mixed to a uniform consistency. After subjection to the high shear forces of the pump the compositions's viscosity began to increase and became stiff after subjection to the spray-applicator. Thus, the dispersion exhibited a high degree of body which adhered well to the steel structure and did not crack or sag while setting to a dry uniform coating.
EXAMPLE II
A gypsum-based composition was prepared by dry mixing the following:
______________________________________                                    
Ingredients           wt. %                                               
______________________________________                                    
Gypsum Plaster        69.2                                                
Perlite (3.9 pcf)     13.9                                                
Shredded Expanded Polystyrene                                             
                      1.8                                                 
(0.375 pcf)                                                               
Cellulose fiber       5.0                                                 
Air-Entraining Agent  0.2                                                 
(alpha olefin sulfonate)                                                  
Sepiolite granules    9.0                                                 
(65% larger than                                                          
325 mesh U.S. Std. with                                                   
average particle size of                                                  
about 140 mesh)                                                           
______________________________________                                    
The dry composition was mixed, pumped, sprayed and applied in the same manner as described in Example I above except that the water/solids ratio was 1.45 and the pump pressure was 185 psi. Viscosity measurements and observations were done as described in Example I above. The results were:
______________________________________                                    
Vicat Viscosity                                                           
               Observations                                               
Mixer Pump    Sprayer  Set  Cracking                                      
                                   Sagging                                
                                          Adhesion                        
______________________________________                                    
26    22      20       Yes  No     No     Yes                             
______________________________________                                    
Again this composition formed a low-viscosity dispersion in the mixer. After subjection to the high-shear pump the viscosity increased and further increased upon application from the sprayer. The resultant high-viscosity dispersion adhered well to the steel beam and set without cracking or sagging.
A second composition was formed in the same manner as described above except that the sepiolite was not present. The initial composition had good viscosity in the mixer but, upon application, was too thin to remain on the steel beam, e.g. it exhibited sagging and poor adhesion.
EXAMPLE III
A dry gypsum-based composition was formed by dry mixing the following:
______________________________________                                    
Ingredients         wt. %                                                 
______________________________________                                    
Gypsum plaster      58.0                                                  
Perlite (3.9 pcf)   23.2                                                  
Cellulose fiber     10.3                                                  
Air-entraining Agent                                                      
                    0.2                                                   
(WITCONATE AOK)                                                           
Attapulgite granules                                                      
                    8.3                                                   
(90% greater than 325 mesh                                                
U.S. Standard; Average                                                    
Particle Size about 140 mesh                                              
______________________________________                                    
The dry mixture was mixed with water (water/solid ratio of 1.7), pumped and spray-applied to a steel I-beam as described in Example I above. Vicat Viscosity measurements and observation of the formed coating were made as described in Example I above. The results are given below:
______________________________________                                    
Vicat Viscosity                                                           
               Observations                                               
Mixer Pump    Sprayer  Set  Cracking                                      
                                   Sagging                                
                                          Adhesion                        
______________________________________                                    
20    20      18       Yes  No     No     Yes                             
______________________________________                                    
The higher density aggregate used here required higher loading of aggregate and, therefore, a predictably more viscous initial dispersion. However, the material was readily mixable to a uniform dispersion which did exhibit the desired rheopectic properties after the pump and sprayer and thereby provided a coating having excellent properties.
EXAMPLE IV
The following example is given for comparative purposes only.
A dry gypsum-based composition was formed by dry mixing the following:
______________________________________                                    
Ingredients        wt. %                                                  
______________________________________                                    
Gypsum plaster     68.8                                                   
Perlite (3.9 pcf)  26.1                                                   
Cellulose fibers   4.9                                                    
Air-entraining Agent                                                      
                   0.2                                                    
(WITCONATE AOK)                                                           
______________________________________                                    
The dry mix was mixed with water (water/solid ratio of 1.4), pumped and spray-applied to a steel I-beam as described in Example 1 above. The following measurements and observations were made as described in Example I.
______________________________________                                    
Vicat Viscosity                                                           
               Observations                                               
Mixer Pump    Sprayer  Set  Cracking                                      
                                   Sagging                                
                                          Adhesion                        
______________________________________                                    
20    32      27       Yes  No     Yes    No                              
______________________________________                                    
The above example shows that when the subject clay rheopetic agent was not present, the composition was thicker (lower number is more viscous) in mixer (harder to mix) and still too thin at the point of application. The resultant coating showed excessive sagging and poor adhesion.

Claims (18)

What is claimed:
1. A dry composition comprising a hydratable cement, porous aggregate particulate, a fibrous material, an air-entraining agent and a magnesium silicate-based clay selected from the group consisting of granular attapulgite, sepiolite or mixtures thereof which have a particle size distribution such that at least 60 weight percent is greater than 44 microns and the average particle size is at least 72 microns; said clay being present in an amount to impart, on addition of water, rheopectic properties to an aqueous dispersion of said composition.
2. The composition of claim 1 having from about 50 to 90 wt. percent cement, from about 3 to 40 vol. percent aggregate, from about 4 to 10 wt. percent organic fibrous material, from 0 to 2 wt. percent of an inorganic fibrous material, from about 0.05 to 0.5 wt. percent air-entraining agent and from about 3 to 20 wt. percent of said clay having a water content of less than about 16 wt. percent.
3. The composition of claim 1 wherein the porous aggregate is a polystyrene selected from the group consisting of shredded expanded polystyrene beads, shredded polystyrene beadboard, shredded extruded polystyrene or mixtures thereof.
4. The composition of claim 3 wherein the shredded polystyrene has a density of from about 0.2 to about 0.8 pcf and is present in from about 1 to 5 weight percent of said composition; and wherein the hydratable cement is gypsum and is present in at least about 75 weight percent of said composition.
5. The composition of claim 1 wherein the porous aggregate is an exfoliated vermiculite.
6. The composition of claim 5 wherein the exfoliated vermiculite has a density of from about 5 to about 7 pcf and is present in from about 20 to about 40 weight percent; and wherein the hydratable cement is a gypsum and is present in from about 50 to about 70 weight percent.
7. The composition of claim 1 wherein the porous aggregate is an expanded perlite having a density of from about 2 to about 12 pcf.
8. The composition of claim 7 wherein the expanded perlite has a density of from about 2 to about 5 pcf and is present in from about 5 to about 30 weight percent; and wherein the hydratable cement is gypsum and is present in from about 50 to about 70 weight percent.
9. The composition of claim 1, 2, 3, 4, 5, 6, 7 or 8 wherein the magnesium silicate-based clay is dried, granulated attapulgite clay wherein at least about 80 weight percent of said granulate has a particle size of at least 44 microns, has a water content of less than about 16 weight percent, and is present in from about 3 to about 10 weight percent in said composition.
10. The composition of claim 1, 2, 3, 4, 5, 6, 7 or 8 wherein the magnesium silicate-based clay is dried, granulated sepiolite clay wherein at least about 60 weight percent of said granulate has a particle size of at least 44 microns, has a water content of less than about 16 weight percent and is present in from about 3 to about 10 weight percent of said composition.
11. The composition of claim 1 having from about 1 to about 5 wt. percent of a shredded polystyrene; at least about 75 weight percent of a hydratable cement composed of hydratable gypsum plaster; fibrous material composed of from about 4 to 10 wt. percent of high wet bulking organic fibers, and from 0 to about 2 wt. percent glass fibers; from about 0.1 to about 0.5 wt. percent of the air-entraining agent; and from about 3 to about 10 wt. percent of the dried, granular magnesium silicate clay.
12. The composition of claim 1 having from about 20 to about 40 wt. percent of an exfoliated vermiculite; at least about 50 weight percent of the hydratable cement composed of a hydratable gypsum plaster; fibrous material composed of from about 4 to about 10 wt. percent of high wet bulking organic fibers, and 0 to 2 wt. percent of glass fibers; from about 0.1 to about 0.5 wt. percent of an air-entraining agent and from about 3 to about 10 wt. percent of a dried, granular magnesium silicate clay.
13. The composition of claim 1 having from about 5 to about 30 wt. percent of an expanded perlite (density of about 2-5 pcf); at least about 50 weight percent of hydratable cement composed of a hydratable gypsum plaster; fibrous material composed of from about 4 to about 15 wt. percent high wet bulking organic fibers, and 0 to about 2 wt. percent glass fibers; from about 0.1 to about 0.5 wt. percent of an air-entraining agent; and from about 3 to about 20 wt. percent of a dried, granular magnesium silicate clay.
14. An aqueous dispersion formed upon the addition of water to the composition of claim 1, 2, 4, 6, 8, 11, 12 or 13 wherein the water to cementitious binder is from about 1.2 to 2.5 and said dispersion exhibits an increase in viscosity after application of high shear forces to said dispersion.
15. A process of providing a fireproofing and/or acoustical insulation to construction metal infrastructure comprising forming an aqueous dispersion from water and dry components comprising from about 50 to about 90 wt. percent of a hydratable cement, about 3 to 40 vol. percent of a porous aggregate selected from vermiculite, perlite or shredded polystyrene, about 4 to 10 wt. percent of an organic fibrous material, 0 to about 2 wt. percent of an inorganic fibrous material, about 0.05 to 0.5 wt. percent of an air-entraining agent and about 3 to 20 wt. percent of a magnesium silicate clay selected from the group consisting of attapulgite, sepiolite or mixtures thereof having particle size distribution such that at least 60 wt. percent is greater than 44 microns and the average particle size is greater than 72 microns; adjusting the water content to have a water to cement ratio of from about 1.2 to 2.5:1; subjecting the formed dispersion to high shear forces to cause the viscosity of said dispersion to increase; and applying the resultant dispersion to a construction infrastructure.
16. The process of claim 15 wherein the initial dispersion has a density of from about 35 to 55 pounds per cubic foot.
17. The process of claim 15 wherein the high shear force is generated by a piston-pump alone or in combination with the spray applicator.
18. The process of claim 15, 16, or 17 wherein the hydratable cement is gypsum; the aggregate is shredded polystyrene; the organic fibrous material is cellulosic material; and said clay has a water content (as the initial dry component) of less than 16 wt. percent.
US07/535,634 1990-06-11 1990-06-11 Sprayable fireproofing composition Expired - Lifetime US5034160A (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
US07/535,634 US5034160A (en) 1990-06-11 1990-06-11 Sprayable fireproofing composition
CA 2027318 CA2027318C (en) 1990-06-11 1990-10-11 Sprayable fireproofing composition
ES91305160T ES2075935T3 (en) 1990-06-11 1991-06-07 FIRE-PROJECTABLE SPRAY-PROOF COMPOSITION.
DE69112290T DE69112290T2 (en) 1990-06-11 1991-06-07 Sprayable, fireproof composition.
EP19910305160 EP0461821B1 (en) 1990-06-11 1991-06-07 Sprayable fireproofing composition
JP16244691A JPH0662325B2 (en) 1990-06-11 1991-06-07 Sprayable fireproof composition
AU78271/91A AU634692B2 (en) 1990-06-11 1991-06-11 Sprayable fireproofing composition
MYPI91001034A MY106678A (en) 1990-06-11 1991-06-11 Sprayable fireproofing composition
KR1019910009698A KR0172125B1 (en) 1990-06-11 1991-06-11 Aprayable fireproofing composition
HK182295A HK182295A (en) 1990-06-11 1995-11-30 Sprayable fireproofing composition

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US07/535,634 US5034160A (en) 1990-06-11 1990-06-11 Sprayable fireproofing composition

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US5556578A (en) * 1993-12-23 1996-09-17 W. R. Grace & Co.-Conn. Aggregate containing hydration water in spray applied fireproofing
US6085470A (en) * 1997-07-02 2000-07-11 Bigelow; William H. Portable building
US6088969A (en) * 1997-07-02 2000-07-18 Porta-Kamp Mfg. Co. Roof and portable building
US6162288A (en) * 1999-05-19 2000-12-19 W. R. Grace & Co.-Conn. Sprayable fireproofing composition
WO2001005591A1 (en) * 1999-07-20 2001-01-25 W.R. Grace & Co.-Conn. High temperature heat transfer barrier and vapor barrier and methods
US6295766B1 (en) * 1999-03-25 2001-10-02 William H. Bigelow Building construction
US6368527B1 (en) * 2000-08-18 2002-04-09 Vladimir Gontmakher Method for manufacture of foamed perlite material
US6406755B1 (en) 1999-01-27 2002-06-18 W.R. Grace & Co.-Conn. Sprayable fireproofing composition
USH2063H1 (en) 2000-03-13 2003-05-06 The United States Of America As Represented By The Secretary Of The Navy Thermal barrier and method of use
US20030099848A1 (en) * 2001-11-20 2003-05-29 Fujio Kondo Fire-proof coating material and fire-proof construction
US6572696B1 (en) * 1998-05-12 2003-06-03 Tolsa, S.A. Technological additive for agglomerating projectable building materials and utilization of the additive in projected mortars and concretes
US20040028904A1 (en) * 2001-01-09 2004-02-12 Jong-Won Park Ultra-light insulation material composition with nonflammability and thermal resistance characteristic, apparatus for manufacturing the same, and method for manufacturing the same by using the apparatus
EP1404626A1 (en) * 2001-07-06 2004-04-07 G-P Gypsum Corporation Fire door components and fire doors comprising the components
US20050183382A1 (en) * 2002-06-06 2005-08-25 Jensen Gary L. Method of making members with a thermal break
US20060281848A1 (en) * 2003-07-17 2006-12-14 Toru Ueno Thixotropy imparting agent
US20070245658A1 (en) * 2004-05-24 2007-10-25 Kevin Yuers Method and System for Constructing a Concrete Waterstop Joint and Use of a Cementitious and Reactive Waterproofing Grout Strip
CN100424029C (en) * 2007-01-29 2008-10-08 袁长兵 Attapulgite insulated brick for sun-light green-house
US20080305554A1 (en) * 2007-06-05 2008-12-11 Hilton Dennis M Automated yield monitoring and control
US7842348B2 (en) 2005-02-04 2010-11-30 W. R. Grace & Co.-Conn. High yield spray application
US20110024702A1 (en) * 2008-03-31 2011-02-03 Barbara Roman Aleman Gypsum mortar with added expanded vermiculite and method for obtaining same
WO2012095562A1 (en) * 2011-01-12 2012-07-19 Acoustic Group Oy Coating and its manufacturing process
EP2559676A1 (en) * 2011-08-16 2013-02-20 Sto Ag Coating composition comprising a mineral binder and a layered silicate and coating system and insulation system comprising a coating material
EP1995407A3 (en) * 2007-05-22 2013-10-02 S & B Industrial Minerals GmbH Method for consolidating and/or sealing loose geological formations in the process of geotechnical construction
ES2515640A1 (en) * 2014-07-18 2014-10-29 Universidad Politécnica de Madrid Procedure for obtaining a plaster-based building material
CN104130634A (en) * 2014-06-27 2014-11-05 苏州市盛百威包装设备有限公司 Coating material used for steel surface, and preparation method thereof
US20150175815A1 (en) * 2012-07-13 2015-06-25 Goodwin Plc Fire retardant paint
US9416052B2 (en) * 2014-04-30 2016-08-16 Active Minerals International, Llc Concrete materials with modified rheology, methods of making, and uses thereof
WO2017077246A1 (en) * 2015-11-03 2017-05-11 Parexgroup Sa Dry construction composition wet-sprayable by means of a screw pump and containing a binder and a biosourced filler, and preparation and uses of such a composition
CN110023264A (en) * 2016-11-03 2019-07-16 派雷斯集团股份公司 The dry composition of this manufacture is used for for multilayer isolation its manufacturing method-of building system-of building
CN110099879A (en) * 2016-11-03 2019-08-06 派雷斯集团股份公司 Can by screw pump wet shot and include the preparation and use of the dry construction composition of binder and biological source filler, the composition

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Cited By (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5556578A (en) * 1993-12-23 1996-09-17 W. R. Grace & Co.-Conn. Aggregate containing hydration water in spray applied fireproofing
US6085470A (en) * 1997-07-02 2000-07-11 Bigelow; William H. Portable building
US6088969A (en) * 1997-07-02 2000-07-18 Porta-Kamp Mfg. Co. Roof and portable building
US6572696B1 (en) * 1998-05-12 2003-06-03 Tolsa, S.A. Technological additive for agglomerating projectable building materials and utilization of the additive in projected mortars and concretes
US6406755B1 (en) 1999-01-27 2002-06-18 W.R. Grace & Co.-Conn. Sprayable fireproofing composition
US6295766B1 (en) * 1999-03-25 2001-10-02 William H. Bigelow Building construction
US6162288A (en) * 1999-05-19 2000-12-19 W. R. Grace & Co.-Conn. Sprayable fireproofing composition
US6309740B1 (en) 1999-07-20 2001-10-30 W. R. Grace & Co.-Conn. High temperature heat transfer barrier and vapor barrier and methods
WO2001005591A1 (en) * 1999-07-20 2001-01-25 W.R. Grace & Co.-Conn. High temperature heat transfer barrier and vapor barrier and methods
USH2063H1 (en) 2000-03-13 2003-05-06 The United States Of America As Represented By The Secretary Of The Navy Thermal barrier and method of use
US6368527B1 (en) * 2000-08-18 2002-04-09 Vladimir Gontmakher Method for manufacture of foamed perlite material
US20040028904A1 (en) * 2001-01-09 2004-02-12 Jong-Won Park Ultra-light insulation material composition with nonflammability and thermal resistance characteristic, apparatus for manufacturing the same, and method for manufacturing the same by using the apparatus
EP1404626A4 (en) * 2001-07-06 2008-03-19 Georgia Pacific Gypsum Llc Fire door components and fire doors comprising the components
EP1404626A1 (en) * 2001-07-06 2004-04-07 G-P Gypsum Corporation Fire door components and fire doors comprising the components
US6730148B2 (en) * 2001-11-20 2004-05-04 Kawaguchi-Mac Industry Co, Ltd Fire-proof coating material and fire-proof construction
US20030099848A1 (en) * 2001-11-20 2003-05-29 Fujio Kondo Fire-proof coating material and fire-proof construction
US20050183382A1 (en) * 2002-06-06 2005-08-25 Jensen Gary L. Method of making members with a thermal break
US20060281848A1 (en) * 2003-07-17 2006-12-14 Toru Ueno Thixotropy imparting agent
US8122677B2 (en) * 2004-05-24 2012-02-28 Khi Capital Inc. Method and system for constructing a concrete waterstop joint and use of a cementitious and reactive waterproofing grout strip
US20070245658A1 (en) * 2004-05-24 2007-10-25 Kevin Yuers Method and System for Constructing a Concrete Waterstop Joint and Use of a Cementitious and Reactive Waterproofing Grout Strip
US8616153B2 (en) 2005-02-04 2013-12-31 W. R. Grace & Co.-Conn. High yield spray application
US7842348B2 (en) 2005-02-04 2010-11-30 W. R. Grace & Co.-Conn. High yield spray application
US20110033628A1 (en) * 2005-02-04 2011-02-10 Michael Abbott High Yield Spray Application
CN100424029C (en) * 2007-01-29 2008-10-08 袁长兵 Attapulgite insulated brick for sun-light green-house
EP1995407A3 (en) * 2007-05-22 2013-10-02 S & B Industrial Minerals GmbH Method for consolidating and/or sealing loose geological formations in the process of geotechnical construction
US8714177B2 (en) 2007-06-05 2014-05-06 W.R. Grace & Co. -Conn. Automated yield monitoring and control
US8206123B2 (en) 2007-06-05 2012-06-26 W. R. Grace & Co.-Conn. Automated yield monitoring and control
US20080305554A1 (en) * 2007-06-05 2008-12-11 Hilton Dennis M Automated yield monitoring and control
US20110024702A1 (en) * 2008-03-31 2011-02-03 Barbara Roman Aleman Gypsum mortar with added expanded vermiculite and method for obtaining same
US8021476B2 (en) * 2008-03-31 2011-09-20 Fire Test, S.L. Gypsum mortar with added expanded vermiculite and method for obtaining same
WO2012095562A1 (en) * 2011-01-12 2012-07-19 Acoustic Group Oy Coating and its manufacturing process
US20140000981A1 (en) * 2011-01-12 2014-01-02 Esa Silfverhuth Coating and its manufacturing process
US9027704B2 (en) * 2011-01-12 2015-05-12 Lumir Oy Coating and its manufacturing process
EP2559676A1 (en) * 2011-08-16 2013-02-20 Sto Ag Coating composition comprising a mineral binder and a layered silicate and coating system and insulation system comprising a coating material
US20150175815A1 (en) * 2012-07-13 2015-06-25 Goodwin Plc Fire retardant paint
US10266706B2 (en) * 2012-07-13 2019-04-23 Goodwin Plc Fire retardant paint
EP3137431A4 (en) * 2014-04-30 2017-12-20 Active Minerals International LLC Concrete materials with modified rheology, methods of making, and uses thereof
US9416052B2 (en) * 2014-04-30 2016-08-16 Active Minerals International, Llc Concrete materials with modified rheology, methods of making, and uses thereof
CN104130634A (en) * 2014-06-27 2014-11-05 苏州市盛百威包装设备有限公司 Coating material used for steel surface, and preparation method thereof
ES2515640A1 (en) * 2014-07-18 2014-10-29 Universidad Politécnica de Madrid Procedure for obtaining a plaster-based building material
GB2557859A (en) * 2015-11-03 2018-06-27 Parexgroup Sa Dry construction composition wet-sprayable by means of a screw pump and containing a binder and a biosourced filler, and preparation and uses of such
CN108349810A (en) * 2015-11-03 2018-07-31 派雷斯集团股份公司 It can wet spray and dry construction composition and its preparation and use containing adhesive and biological source filler by screw pump
ES2676912R1 (en) * 2015-11-03 2018-09-21 Parexgroup Sa COMPOSITION OF DRY CONSTRUCTION PROJECTABLE IN WETWAY WITH THE HELP OF A SCREW PUMP AND THAT INCLUDES A BINDING AND A LOAD OF BIOLOGICAL ORIGIN - PREPARATION AND APPLICATION OF SUCH COMPOSITION
WO2017077246A1 (en) * 2015-11-03 2017-05-11 Parexgroup Sa Dry construction composition wet-sprayable by means of a screw pump and containing a binder and a biosourced filler, and preparation and uses of such a composition
US11845696B2 (en) 2015-11-03 2023-12-19 Parexgroup Sa Dry construction composition wet-sprayable by means of a screw pump and containing a binder and a biosourced filler, and preparation and uses of such a composition
CN110023264A (en) * 2016-11-03 2019-07-16 派雷斯集团股份公司 The dry composition of this manufacture is used for for multilayer isolation its manufacturing method-of building system-of building
CN110099879A (en) * 2016-11-03 2019-08-06 派雷斯集团股份公司 Can by screw pump wet shot and include the preparation and use of the dry construction composition of binder and biological source filler, the composition

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EP0461821B1 (en) 1995-08-23
AU634692B2 (en) 1993-02-25
MY106678A (en) 1995-07-31
JPH0662325B2 (en) 1994-08-17
CA2027318C (en) 1998-06-30
DE69112290T2 (en) 1996-03-14
CA2027318A1 (en) 1991-12-12
HK182295A (en) 1995-12-08
KR920000881A (en) 1992-01-29
ES2075935T3 (en) 1995-10-16
AU7827191A (en) 1991-12-12
KR0172125B1 (en) 1999-03-20
DE69112290D1 (en) 1995-09-28
JPH04228461A (en) 1992-08-18
EP0461821A1 (en) 1991-12-18

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